2016
DOI: 10.1177/0004867416637920
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Associations of 5HTTLPR polymorphism with major depressive disorder and alcohol dependence: A systematic review and meta-analysis

Abstract: Our meta-analysis confirms that individuals with the homozygous S allele of 5HTTLPR polymorphism are at increased risks of major depressive disorder as well as alcohol dependence. Further studies are required to investigate the association between 5HTTLPR polymorphism and the comorbidity of major depressive disorder and alcohol dependence as well as gene × environmental interactions.

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Cited by 38 publications
(20 citation statements)
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“…Most research notes the association between alcohol and depression, and a genetic basis was identified for this occurrence. In a meta-analysis, Oo et al 26 confirm that individuals with homozygous S allele of the 5HTTLPR polymorphism have increased risk of major depression and alcohol addiction.…”
Section: Discussionmentioning
confidence: 99%
“…Most research notes the association between alcohol and depression, and a genetic basis was identified for this occurrence. In a meta-analysis, Oo et al 26 confirm that individuals with homozygous S allele of the 5HTTLPR polymorphism have increased risk of major depression and alcohol addiction.…”
Section: Discussionmentioning
confidence: 99%
“…Homozygous and heterozygous carriers of the short allele variant were found to be at increased risk of major depressive disorder. Notably, homozygous carriers of the short allele are also at increased risk for alcohol dependence (60), lending an interesting biological footprint to the association between AUDs, depression, and suicide in men. Examining the concomitant effects of another polymorphism (C1019G) from the serotonin receptor gene, 5HT1A and the Val66Met polymorphism of the BDNF gene revealed increased risk for depression when expressing both risk variants (61).…”
Section: Genetic Risk Constellationmentioning
confidence: 99%
“…The analysis of the association between the 5-HTTLPR polymorphism and neuropsychiatric disorders, including anxiety and depressive syndromes, has shown some positive but contradictory findings. Significant associations between the short variant and susceptibility for mood disorders have been reported [ 26 , 27 , 28 ] but other studies did not confirm these findings [ 29 ]. The original results of Caspi et al [ 30 ] suggested that individuals carrying the short ( s ) allele are more likely to develop major depression following exposure to early life stress (e.g., childhood maltreatment).…”
Section: Introductionmentioning
confidence: 99%